BEUDAMED
    FDA Recall Open, Classified

    Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System

    Recall: Z-2282-2026 · Initiated May 6, 2026

    Recall

    Recall Number
    Z-2282-2026
    Event Number
    98894
    Firm
    Stryker Corporation
    FEI Number
    3015967359
    Product Code
    JCX
    Status
    Open, Classified
    Root Cause
    Nonconforming Material/Component
    Initiated
    May 6, 2026
    Posted
    June 1, 2026
    Address
    1941 Stryker Way, Portage, MI, 49002-9711

    Description

    Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System

    Reason

    It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a potential risk of electrical shock due to the device s safety testing being unverifiable.

    Action

    Stryker issued an URGENT Medical Device Field Action notice to its consignee on 5/6/2026 via FedEx. The notice explained the issue, potential risk and requested the consignee locate and quarantine the device. The consignee was directed to contact their Stryker Sales Rep to help schedule replacement of the affected device. For questions of concerns, contact Brooke Thompson at [email protected].

    Distribution

    US Nationwide distribution in the state of Indiana.

    Quantity

    1 unit